Jarius S, Wildemann B, Stöcker W, Moser A, Wandinger K P
Molecular Neuroimmunology Group, Department of Neurology, University of Heidelberg, Heidelberg, Germany.
Molecular Neuroimmunology Group, Department of Neurology, University of Heidelberg, Heidelberg, Germany.
J Neuroimmunol. 2015 Sep 15;286:79-82. doi: 10.1016/j.jneuroim.2015.07.009. Epub 2015 Jul 22.
Antibodies to the Rho GTPase-activating protein 26 (ARHGAP26, GRAF1) (also termed anti-Ca) were first described in patients with cerebellar ataxia. However, ARHGAP26 is also expressed in some hippocampal neurons. Moreover, some of the previously reported patients showed cognitive and affective symptoms. It is unknown whether those symptoms reflected involvement of the limbic system or were part of the so-called cerebellar cognitive/affective syndrome.
Here, we report a newly diagnosed anti-Ca/ARHGAP26-IgG-positive patient who presented with recurrent psychotic symptoms but no cerebellar ataxia. In addition, low-titer acetylcholine receptor antibodies, voltage-gated potassium channel complex antibodies (but no LGI1 or CASPR2 antibodies) and anti-nuclear antibodies of unknown specificity were detected, suggesting a general autoimmune predisposition. Thymectomy revealed mild thymic nodular hyperplasia.
This case indicates that the clinical spectrum of ARHGAP26-related autoimmunity might be broader than expected. Studies on the prevalence of anti-Ca/ARHGAP26 in patients with suspected limbic encephalitis seem warranted.
针对Rho GTP酶激活蛋白26(ARHGAP26,GRAF1)(也称为抗Ca)的抗体最初在小脑共济失调患者中被描述。然而,ARHGAP26也在一些海马神经元中表达。此外,一些先前报道的患者表现出认知和情感症状。尚不清楚这些症状是反映了边缘系统受累还是所谓的小脑认知/情感综合征的一部分。
在此,我们报告一名新诊断的抗Ca/ARHGAP26-IgG阳性患者,该患者出现反复的精神病性症状但无小脑共济失调。此外,检测到低滴度的乙酰胆碱受体抗体、电压门控钾通道复合物抗体(但无LGI1或CASPR2抗体)以及特异性未知的抗核抗体,提示存在一般自身免疫易感性。胸腺切除术显示轻度胸腺结节性增生。
该病例表明ARHGAP26相关自身免疫的临床谱可能比预期更广。对疑似边缘性脑炎患者中抗Ca/ARHGAP26患病率的研究似乎很有必要。